Agency Forms Undergoing Paperwork Reduction Act Review, 4987-4988 [2020-01378]
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Federal Register / Vol. 85, No. 18 / Tuesday, January 28, 2020 / Notices
Request for Comments
In accordance with the Paperwork
Reduction Act of 1995, 44 U.S.C. 3501–
3521, comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) Whether the
proposed collection of information is
necessary for the proper performance of
AHRQ health care research and health
care information dissemination
functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) of
information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: January 22, 2020.
Virginia L. Mackay-Smith,
Associate Director.
[FR Doc. 2020–01385 Filed 1–27–20; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–0822]
jbell on DSKJLSW7X2PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘The National
Intimate Partner and Sexual Violence
Survey (NISVS)’’ to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on October 9,
2019 to obtain comments from the
public and affected agencies. CDC
received two anonymous nonsubstantive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
VerDate Sep<11>2014
17:02 Jan 27, 2020
Jkt 250001
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
The National Intimate Partner and
Sexual Violence Survey (NISVS) (OMB
Control No. 0920–0822, Exp. 02/29/
2020)—Revision—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
This is a revision request for the
currently approved National Intimate
Partner and Sexual Violence Survey
(NISVS, OMB# 0920–0822). In 2010, the
National Intimate Partner and Sexual
Violence Surveillance System (NISVS)
reported that approximately 6.9 million
women and 5.6 million men
experienced rape, physical violence
and/or stalking by an intimate partner
within the last year. The health care
costs of IPV exceed $5.8 billion each
year, nearly $3.9 billion of which is for
direct medical and mental health care
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4987
services. In order to address this
important public health problem, CDC
implemented, beginning in 2010, the
National Intimate Partner and Sexual
Violence Surveillance System that
produces national and state level
estimates of Intimate Partner Violence
(IPV), Sexual Violence (SV) and stalking
on an annual basis.
This revision request describes the
planned testing of a redesign of the
National Intimate Partner and Sexual
Violence Survey (NISVS) and the
approach for collecting NISVS data
using multiple data collection modes
and sampling strategies. More
specifically, this revision request is to;
(1) Conduct feasibility testing to assess
several alternative design features,
including the sample frame (addressbased sample [ABS], random digit dial
[RDD], web panel), mode of response
(telephone, web, paper), and incentive
structures that help garner participation
and help reduce nonresponse. (2)
Conduct experiments that inform the
development of a protocol for
alternative sampling and weighting
methods for multi-modal data collection
that will result in the ability to calculate
accurate and reliable national and statelevel estimates of SV, IPV, and stalking,
and (3) Conduct a pilot data collection
to ensure that the selected optimal
alternative sampling methods and
multi-modal data collection approaches
for NISVS are ready for full-scale
implementation.
These data will be used only to
inform future NISVS data collections.
Results from the feasibility phase
experiments may be prepared for
publication, as the findings related to
optimal data collection modes, sampling
frames, and incentive structures are
likely to be useful to other federal
agencies currently conducting national
data collections. No national prevalence
estimates will be generated from the
data collected during the NISVS
redesign project. The feasibility study
involves testing of the CATI, paper, and
web versions of the NISVS survey using
a variety of sampling frames and single
vs. multiple modes, all for the purpose
of determining a new design for NISVS,
and the pilot test of the new design.
Data are analyzed using appropriate
statistical software to account for the
complexity of the survey design to
compute weighted counts, percentages,
and confidence intervals using nationallevel data.
OMB approval is requested for three
years. The total estimated annualized
burden hours are 1,189. There is no cost
to respondents other than their time.
E:\FR\FM\28JAN1.SGM
28JAN1
4988
Federal Register / Vol. 85, No. 18 / Tuesday, January 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Individuals and
Households.
Average
burden per
response
(in hours)
958
1
3/60
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
333
389
389
667
427
211
29
667
40
27
27
14
13
22
29
14
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3/60
3/60
3/60
40/60
25/60
25/60
40/60
25/60
1
3/60
3/60
3/60
3/60
40/60
25/60
25/60
40/60
2 Screener—ABS, web ...............................................................
2 Screener—ABS, paper—Roster method .................................
2 Screener—ABS, paper—YMOF Method .................................
2 Questionnaire—RDD (CATI) ....................................................
2—Questionnaire—ABS, web .....................................................
2 Questionnaire—ABS, paper .....................................................
2 Questionnaire—ABS, in-bound CATI ......................................
2 Questionnaire—Panel, web .....................................................
2 Cognitive Testing Protocol—Cognitive testing ........................
3 Screener—RDD (CATI) ...........................................................
3 Screener—ABS, web ...............................................................
3 Screener—ABS, paper—Roster method .................................
3 Screener ABS, paper—YMOF Method ....................................
3 Questionnaire—RDD (CATI) ....................................................
3 Questionnaire—ABS, web .......................................................
3 Questionnaire—ABS, paper .....................................................
3 Questionnaire—ABS, in-bound CATI ......................................
[FR Doc. 2020–01378 Filed 1–27–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–20EU; Docket No. CDC–2019–
0119]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Capacity Building Assistance
Program: Data Management, Monitoring,
and Evaluation. The purpose of this data
collection is to evaluate the CDC
cooperative agreement program entitled
CDC–RFA–PS19–1904: Capacity
SUMMARY:
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Number of
responses per
respondent
Phase 2 Screener—RDD (CATI) ...........................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
VerDate Sep<11>2014
Number of
respondents
Form name
17:02 Jan 27, 2020
Jkt 250001
Building Assistance (CBA) for High
Impact HIV Prevention Program
Integration.
DATES: CDC must receive written
comments on or before March 30, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0119 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
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requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Capacity Building Assistance
Program: Data Management, Monitoring,
E:\FR\FM\28JAN1.SGM
28JAN1
]]>Agencies
[Federal Register Volume 85, Number 18 (Tuesday, January 28, 2020)]
[Notices]
[Pages 4987-4988]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01378]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-0822]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``The National Intimate Partner and Sexual
Violence Survey (NISVS)'' to the Office of Management and Budget (OMB)
for review and approval. CDC previously published a ``Proposed Data
Collection Submitted for Public Comment and Recommendations'' notice on
October 9, 2019 to obtain comments from the public and affected
agencies. CDC received two anonymous non-substantive comments related
to the previous notice. This notice serves to allow an additional 30
days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to [email protected]. Direct written comments
and/or suggestions regarding the items contained in this notice to the
Attention: CDC Desk Officer, Office of Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by fax to (202) 395-5806. Provide
written comments within 30 days of notice publication.
Proposed Project
The National Intimate Partner and Sexual Violence Survey (NISVS)
(OMB Control No. 0920-0822, Exp. 02/29/2020)--Revision--National Center
for Injury Prevention and Control (NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This is a revision request for the currently approved National
Intimate Partner and Sexual Violence Survey (NISVS, OMB# 0920-0822). In
2010, the National Intimate Partner and Sexual Violence Surveillance
System (NISVS) reported that approximately 6.9 million women and 5.6
million men experienced rape, physical violence and/or stalking by an
intimate partner within the last year. The health care costs of IPV
exceed $5.8 billion each year, nearly $3.9 billion of which is for
direct medical and mental health care services. In order to address
this important public health problem, CDC implemented, beginning in
2010, the National Intimate Partner and Sexual Violence Surveillance
System that produces national and state level estimates of Intimate
Partner Violence (IPV), Sexual Violence (SV) and stalking on an annual
basis.
This revision request describes the planned testing of a redesign
of the National Intimate Partner and Sexual Violence Survey (NISVS) and
the approach for collecting NISVS data using multiple data collection
modes and sampling strategies. More specifically, this revision request
is to; (1) Conduct feasibility testing to assess several alternative
design features, including the sample frame (address-based sample
[ABS], random digit dial [RDD], web panel), mode of response
(telephone, web, paper), and incentive structures that help garner
participation and help reduce nonresponse. (2) Conduct experiments that
inform the development of a protocol for alternative sampling and
weighting methods for multi-modal data collection that will result in
the ability to calculate accurate and reliable national and state-level
estimates of SV, IPV, and stalking, and (3) Conduct a pilot data
collection to ensure that the selected optimal alternative sampling
methods and multi-modal data collection approaches for NISVS are ready
for full-scale implementation.
These data will be used only to inform future NISVS data
collections. Results from the feasibility phase experiments may be
prepared for publication, as the findings related to optimal data
collection modes, sampling frames, and incentive structures are likely
to be useful to other federal agencies currently conducting national
data collections. No national prevalence estimates will be generated
from the data collected during the NISVS redesign project. The
feasibility study involves testing of the CATI, paper, and web versions
of the NISVS survey using a variety of sampling frames and single vs.
multiple modes, all for the purpose of determining a new design for
NISVS, and the pilot test of the new design. Data are analyzed using
appropriate statistical software to account for the complexity of the
survey design to compute weighted counts, percentages, and confidence
intervals using national-level data.
OMB approval is requested for three years. The total estimated
annualized burden hours are 1,189. There is no cost to respondents
other than their time.
[[Page 4988]]
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Individuals and Households...................... Phase 2 Screener--RDD (CATI).......................... 958 1 3/60
Phase 2 Screener--ABS, web............................ 333 1 3/60
Phase 2 Screener--ABS, paper--Roster method........... 389 1 3/60
Phase 2 Screener--ABS, paper--YMOF Method............. 389 1 3/60
Phase 2 Questionnaire--RDD (CATI)..................... 667 1 40/60
Phase 2--Questionnaire--ABS, web...................... 427 1 25/60
Phase 2 Questionnaire--ABS, paper..................... 211 1 25/60
Phase 2 Questionnaire--ABS, in-bound CATI............. 29 1 40/60
Phase 2 Questionnaire--Panel, web..................... 667 1 25/60
Phase 2 Cognitive Testing Protocol--Cognitive testing. 40 1 1
Phase 3 Screener--RDD (CATI).......................... 27 1 3/60
Phase 3 Screener--ABS, web............................ 27 1 3/60
Phase 3 Screener--ABS, paper--Roster method........... 14 1 3/60
Phase 3 Screener ABS, paper--YMOF Method.............. 13 1 3/60
Phase 3 Questionnaire--RDD (CATI)..................... 22 1 40/60
Phase 3 Questionnaire--ABS, web....................... 29 1 25/60
Phase 3 Questionnaire--ABS, paper..................... 14 1 25/60
Phase 3 Questionnaire--ABS, in-bound CATI............. 2 1 40/60
--------------------------------------------------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-01378 Filed 1-27-20; 8:45 am]
BILLING CODE 4163-18-P
